SU591118A3 - Композици дл регулировани роста растений - Google Patents
Композици дл регулировани роста растенийInfo
- Publication number
- SU591118A3 SU591118A3 SU752121786A SU2121786A SU591118A3 SU 591118 A3 SU591118 A3 SU 591118A3 SU 752121786 A SU752121786 A SU 752121786A SU 2121786 A SU2121786 A SU 2121786A SU 591118 A3 SU591118 A3 SU 591118A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- growth
- dihydro
- phenyl
- oxathiine
- plants
- Prior art date
Links
- 230000012010 growth Effects 0.000 title description 17
- 239000000203 mixture Substances 0.000 title description 9
- 230000033228 biological regulation Effects 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims description 11
- 101000993347 Gallus gallus Ciliary neurotrophic factor Proteins 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 235000014121 butter Nutrition 0.000 description 8
- 241001483078 Phyto Species 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 239000004009 herbicide Substances 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 244000068988 Glycine max Species 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 230000008635 plant growth Effects 0.000 description 3
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 3
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 2
- 235000016068 Berberis vulgaris Nutrition 0.000 description 2
- 241000335053 Beta vulgaris Species 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- 231100000674 Phytotoxicity Toxicity 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 125000003944 tolyl group Chemical group 0.000 description 2
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
- 244000144730 Amygdalus persica Species 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 235000004035 Cryptotaenia japonica Nutrition 0.000 description 1
- 206010053759 Growth retardation Diseases 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 235000006040 Prunus persica var persica Nutrition 0.000 description 1
- 206010039897 Sedation Diseases 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- 241001385887 Tachys Species 0.000 description 1
- 102000007641 Trefoil Factors Human genes 0.000 description 1
- 235000015724 Trifolium pratense Nutrition 0.000 description 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 208000035269 cancer or benign tumor Diseases 0.000 description 1
- 239000003433 contraceptive agent Substances 0.000 description 1
- 230000002254 contraceptive effect Effects 0.000 description 1
- 235000019788 craving Nutrition 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 244000037666 field crops Species 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 231100000001 growth retardation Toxicity 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 229920002113 octoxynol Polymers 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000036280 sedation Effects 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D327/00—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
- C07D327/02—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms one oxygen atom and one sulfur atom
- C07D327/06—Six-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/459,442 US3947264A (en) | 1974-04-09 | 1974-04-09 | Substituted 2,3-dihydro-,4-oxathiin plant growth stunting agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU591118A3 true SU591118A3 (ru) | 1978-01-30 |
Family
ID=23824789
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU752121786A SU591118A3 (ru) | 1974-04-09 | 1975-04-09 | Композици дл регулировани роста растений |
Country Status (15)
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4340747A (en) * | 1975-08-15 | 1982-07-20 | Ciba-Geigy Corporation | Esters of 1,2-diphenyl-cyclohex-1-ene-4-carboxylic-acid |
| US4229207A (en) * | 1975-08-15 | 1980-10-21 | Ciba-Geigy Corporation | Esters of 1,2-diphenyl-cyclohex-1-ene-4-carboxylic acid |
| US4340415A (en) * | 1975-08-15 | 1982-07-20 | Ciba-Geigy Corporation | Esters of 1,2-diphenyl-cyclohex-1-ene-4-carboxylic-acid |
| US4127402A (en) * | 1975-10-30 | 1978-11-28 | Uniroyal, Inc. | Substituted 2,3-dihydro-1,4-oxathiin plant growth regulants |
| US4319031A (en) * | 1976-02-06 | 1982-03-09 | Stauffer Chemical Company | Substituted thiazolidines |
| FR2347273A1 (fr) * | 1976-04-06 | 1977-11-04 | Oreal | Opercule muni d'un dispositif d'inviolabilite pour le bouchage d'un recipient |
| CA1130297A (en) * | 1980-05-02 | 1982-08-24 | Michael A. Puttock | Method of making 2,3-dihydro-5,6-diphenyl- 1,4-oxathiin |
| CA1150284A (en) * | 1980-12-02 | 1983-07-19 | Allan K.S. Tsai | Method of making certain 2,3-dihydro-1,4-dithiins |
| US5578498A (en) * | 1991-05-22 | 1996-11-26 | Behringwerke Ag | Metal chelate containing compositions for use in chemiluminescent assays |
| CN107439565A (zh) * | 2017-08-24 | 2017-12-08 | 长沙理工大学 | 一种肾蕨矮控剂及其使用方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3066149A (en) * | 1958-07-30 | 1962-11-27 | Diamond Alkali Co | 1, 3, 5-trithiane compounds |
| US3082214A (en) * | 1958-09-04 | 1963-03-19 | Diamond Alkali Co | Chemical compositions and process |
| US3454391A (en) * | 1966-05-04 | 1969-07-08 | Uniroyal Inc | Stimulation of plant growth |
| DE1957859A1 (de) * | 1969-11-18 | 1971-05-27 | Degussa | Verfahren zur Herstellung von 2,3-Dihydro-p-oxathiinen und deren Sulfoxiden und Sulfonen |
| US3806332A (en) * | 1970-03-09 | 1974-04-23 | Uniroyal Ltd | Plant air pollution protectants |
-
1974
- 1974-04-09 US US05/459,442 patent/US3947264A/en not_active Expired - Lifetime
- 1974-09-04 CA CA208,416A patent/CA1033187A/en not_active Expired
-
1975
- 1975-03-24 GB GB12099/75A patent/GB1499418A/en not_active Expired
- 1975-03-25 DE DE19752513202 patent/DE2513202A1/de not_active Ceased
- 1975-04-01 AR AR258212A patent/AR214965A1/es active
- 1975-04-03 AT AT253375A patent/AT339929B/de not_active IP Right Cessation
- 1975-04-04 NL NL7504007A patent/NL7504007A/xx not_active Application Discontinuation
- 1975-04-06 IL IL47024A patent/IL47024A/xx unknown
- 1975-04-08 FR FR7510932A patent/FR2267038B1/fr not_active Expired
- 1975-04-08 JP JP50042709A patent/JPS50140630A/ja active Pending
- 1975-04-08 DK DK148975A patent/DK148975A/da not_active IP Right Cessation
- 1975-04-08 IT IT67904/75A patent/IT1036206B/it active
- 1975-04-09 CH CH452775A patent/CH614708A5/xx not_active IP Right Cessation
- 1975-04-09 SU SU752121786A patent/SU591118A3/ru active
- 1975-04-09 DD DD185340A patent/DD116737A5/xx unknown
-
1977
- 1977-07-19 AR AR268485A patent/AR223135A1/es active
Also Published As
| Publication number | Publication date |
|---|---|
| IL47024A0 (en) | 1975-06-25 |
| AR214965A1 (es) | 1979-08-31 |
| DK148975A (enrdf_load_stackoverflow) | 1975-10-10 |
| US3947264A (en) | 1976-03-30 |
| DE2513202A1 (de) | 1975-10-23 |
| AT339929B (de) | 1977-11-10 |
| FR2267038B1 (enrdf_load_stackoverflow) | 1977-04-15 |
| JPS50140630A (enrdf_load_stackoverflow) | 1975-11-11 |
| DD116737A5 (de) | 1975-12-12 |
| ATA253375A (de) | 1977-03-15 |
| GB1499418A (en) | 1978-02-01 |
| IL47024A (en) | 1979-05-31 |
| NL7504007A (nl) | 1975-10-13 |
| IT1036206B (it) | 1979-10-30 |
| FR2267038A1 (enrdf_load_stackoverflow) | 1975-11-07 |
| AU7924975A (en) | 1976-09-23 |
| CA1033187A (en) | 1978-06-20 |
| AR223135A1 (es) | 1981-07-31 |
| CH614708A5 (enrdf_load_stackoverflow) | 1979-12-14 |
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